Fuel cell stack

ABSTRACT

Solid oxide fuel cell stack obtainable by a process comprising the use of a glass sealant with composition 50-70 wt % SiO 2 , 0-20 wt % Al 2 O 3 , 10-50 wt % CaO, 0-10 wt % MgO, 0-2 wt % (Na 2 O+K 2 O), 5-10 wt % B 2 O 3 , and 0-5 wt % of functional elements selected from TiO 2 , ZrO 2 , F, P 2 O 5 , MoO 3 , Fe 2 O 3 , MnO 2 , La—Sr—Mn—O perovskite (LSM) and combinations thereof.

The present invention concerns a process for a preparing a Solid OxideFuel Cell (SOFC) stack in which the fuel cell units and interconnectplates making up the stack are provided with a glass sealant having aTEC significantly lower than the rest of the fuel cell prior tooperation. The gas sealant is provided as a thin sheet of paste or glassfibres having a composition within the system comprisingCaO—MgO—SiO₂—Al₂O₃—B₂O₃. More specifically, the invention concerns asolid oxide fuel cell stack obtainable by a process comprising the useof a glass sealant with composition 50-70 wt % SiO₂, 0-20 wt % Al₂O₃,10-50 wt % CaO, 0-10 wt % MgO, 0-2 wt % (Na₂O+K₂O), 5-10 wt % B₂O₃, and0-5 wt % of functional elements selected from TiO₂, ZrO₂, F, P₂O₅, MoO₃,Fe₂O₃, MnO₂, La—Sr—Mn—O perovskite (LSM) and combinations thereof. Theglass sealant is preferably a thin sheet of glass fibres in the form ofE-glass.

A SOFC comprises an oxygen-ion conducting electrolyte, a cathode whereoxygen is reduced and an anode where hydrogen is oxidised. The overallreaction in a SOFC is that hydrogen and oxygen electrochemically reactto produce electricity, heat and water. The operating temperature for aSOFC is in the range 600 to 1000° C., often 650 to 1000° C., more often750 to 850° C. A SOFC delivers in normal operation a voltage of normallybelow about 0.75V. The fuel cells are therefore assembled in stacks inwhich the fuel cells are electrically connected via interconnectorplates.

Typically, such fuel cells are composed of Y-stabilized zirconia (YSZ)electrolyte together with cathode and anode electrodes and contactlayers to the electron conducting interconnect plate. The interconnectmakes the series connection between the cells and is normally providedwith gas supply channels for the fuel cell. Gas-tight sealants are alsousually provided to avoid the mixing of air from the cathode region andfuel from the anode region and they provide also for the proper bondingof the fuel cell units with the interconnector plates. The sealants arethus vitally important for the performance, durability and safeoperation of the fuel cell stacks.

During operation the SOFC is subjected to thermal cycling and maythereby be exposed to tensile stress. If the tensile stress exceeds thetensile strength of the fuel cell, it will crack and the whole fuel cellstack will malfunction. One source of tensile stress in the SOFC arisesfrom the discrepancies between the thermal expansion coefficients (TEC)of the cell stack components. The high operating temperature and thermalcycling of a SOFC stack require that the interconnect plates are made ofmaterials which have a TEC similar to that of the fuel cell units. It istoday possible to find suitable materials for interconnect plates whichhave substantially the same TEC as the cells.

Another source of tensile stress which is more difficult to avoidresults from the discrepancy in TEC of the sealant, often a glasssealant, with respect to the interconnect plates and the cells in thefuel cell stack. It is normally recognized that the thermal expansioncoefficient (TEC) of the sealant should be in the range 11-13·10⁻⁶K⁻¹(25-900° C.), thus corresponding to the TEC of the interconnector plateand/or the fuel cell in order eliminate cracks formation in the fuelcell components. Furthermore, the sealing material has to be stable overa time span of say 40,000 h without reacting with the other materialsand/or ambient gasses.

A common material used in gas-tight sealants is glass of varyingcompositions and much work has been concentrated on development ofsuitable glass compositions:

Our EP-A-1,010,675 describes a number of glass sealing materialssuitable for SOFC, including alkaline oxide silicate glasses, mica glassceramics, alkaline-earth oxide borosilicate/silicaborate glasses andalkaline-earth alumina silicates. This citation teaches the preparationof a glass sealing material based on dried glass powder and a fillermaterial. The TEC of the glass powder may be as low as 7.5·10⁻⁶ K⁻¹ andaccordingly, filler material is added to increase the TEC in the finalglass powder so that it substantially matches that of the interconnectorplates and fuel cell units having TEC of 9-13·10⁻⁶K⁻¹.

EP-A-1,200,371 describes a glass-ceramic composition which is providedas a blend of Al₂O₃, BaO, CaO, SrO, B₂O₃ and SiO₂ within specificranges. The glass and crystallized (after heat treatment) glass-ceramicshow TEC ranging from 7·10⁻⁶ K⁻¹ to 13·10⁻⁶ K⁻¹. However, a considerableamount of BaO is required in the glass ceramic composition to obtain thehigh TEC. Prior to heat treatment, the TEC of the glass-ceramicsubstantially matches that of the other solid ceramic components (within30%).

S. Taniguchi et al. Journal of Power Sources 90 (2000) 163-169 describesthe use of a silica/alumina (52 wt % SiO₂, 48 wt % Al₂O₃; FIBERFRAX® FFXpaper #300, Toshiba Monofrax, thickness 0.35 mm) ceramic fiber assealing material in solid oxide fuel cells. This sealant is able tosuppress electrolyte-cracks in the fuel cell but the sealant propertiesare insufficient, as gas leakage is detected near the sealing material.

US-A-2003/0203267 discloses the use of multilayer seals including theuse of a glass material containing 58% SiO₂, about 9% B₂O₃, about 11%Na₂O, about 6% Al₂O₃, about 4% BaO, and ZnO, CaO and K₂O.

It is an object of the present invention to provide a solid oxide fuelcell stack containing a gas-tight sealant which does not initiatecracking in the cells and which has low reactivity with other cell stackcomponents.

It is another object of the invention to provide a solid oxide fuel cellstack containing a gas-tight sealant which enables faster production ofthe stacks with better thickness tolerance of the sealant across thestack.

It is yet another object of the invention to provide a solid oxide fuelcell stack containing a gas-tight sealant which enables low electricalconductivity at the operation temperature of the stack.

These and other objects are solved by the invention.

Accordingly, we provide a solid oxide fuel cell stack obtainable by aprocess comprising the steps of:

(a) forming a first fuel cell stack assembly by alternating at least oneinterconnector plate with at least one fuel cell unit, in which eachfuel cell unit comprises an anode, a cathode and an electrolyte arrangedbetween the anode and cathode, and providing a glass sealant in betweenthe interconnector plate and each fuel cell unit, in which the glasssealant has the composition:50-70 wt % SiO₂, 0-20 wt % Al₂O₃, 10-50 wt % CaO, 0-10 wt % MgO, 0-2 wt% (Na₂O+K₂O), 5-10 wt % B₂O₃, and 0-5 wt % of functional elementsselected from TiO₂, ZrO₂, F, P₂O₅, MoO₃, Fe₂O₃, MnO₂, La—Sr—Mn—Operovskite (LSM) and combinations thereof;(b) converting said first fuel cell stack assembly into a secondassembly having a glass sealant of thickness 5-100 μm by heating saidfirst assembly to a temperature of 500° C. or higher and subjecting thecell stack to a load pressure of 2 to 20 kg/cm²;(c) converting said second assembly into a final fuel cell stackassembly by cooling the second assembly of step (b) to a temperaturebelow that of step (b).

Preferably in step (b) the temperature is 800° C. or higher and the loadpressure is 2 to 10 kg/cm². Hence, in a preferred embodiment we providea solid oxide fuel cell stack obtainable by a process comprising thesteps of:

(a) forming a first fuel cell stack assembly by alternating at least oneinterconnector plate with at least one fuel cell unit, in which eachfuel cell unit comprises an anode, a cathode and an electrolyte arrangedbetween the anode and cathode, and providing a glass sealant in betweenthe interconnector plate and each fuel cell unit, in which the glasssealant has the composition:50-70 wt % SiO₂, 0-20 wt % Al₂O₃, 10-50 wt % CaO, 0-10 wt % MgO, 0-2 wt% (Na₂O+K₂O), 5-10 wt % B₂O₃, and 0-5 wt %6 of functional elementsselected from TiO₂, ZrO₂, F, P₂O₅, MoO₃, Fe₂O₃, MnO₂, La—Sr—Mn—Operovskite (LSM) and combinations thereof;(b) converting said first fuel cell stack assembly into a secondassembly having a glass sealant of thickness 5-100 μm by heating saidfirst assembly to a temperature of 800° C. or higher and subjecting thecell stack to a load pressure of 2 to 10 kg/cm²;(c) converting said second assembly into a final fuel cell stackassembly by cooling the second assembly of step (b) to a temperaturebelow that of step (b).

In this specification the terms “glass sealant” and “gas-tight sealant”are used interchangeably.

The stack of step (c) may for instance be cooled to room temperature. Byroom temperature (RT) is meant the ambient temperature at which thefirst fuel cell stack assembly is prepared, normally 20-30° C.

By heating said first fuel cell stack assembly to a temperature of 800°C. or higher, such as 850° C., 900° C., 950° C. or higher and at thesame time pressing the cell stack with a load pressure (tighteningpressure) of 2-10 kg/cm², preferably 4-8 kg/cm², it is possible tosqueeze the sealant material so as to form a tight and dense sealant.Still, the load pressure may be higher than 10 kg/cm², for instance upto 20 kg/cm², such as 14 or 18 kg/cm². Preferably, the temperature instep (b) is in the range 800-900° C. Yet, instead of heating to 800° C.or higher, lower temperatures may be used, such as temperatures in therange 500-800° C., such as 550, 600, 650, 700 or 750° C. The closedporous structure thus obtained renders the sealant less susceptible toleakage. The resulting thickness of the sealant is in the range 5 to 100μm, often 5 to 50 μm, more often 10 to 35 μm.

In another preferred embodiment the glass sealant has the composition:

50-65 wt % SiO₂, 0-20 wt % Al₂O₃, 15-40 wt % CaO, 0-10 wt % MgO, 0-2 wt% (Na₂O+K₂O), 5-10 wt % B₂O₃, and 0-5 wt % of functional elementsselected from TiO₂, ZrO₂, F, P₂O₅, MoO₃, Fe₂O₃, MnO₂, La—Sr—Mn—Operovskite (LSM) and combinations thereof.

It would be understood that the glass sealant composition may be free ofAl₂O₃ (0 wt %), but preferably it contains up to 20 wt % Al₂O₃, such as10-15 wt % Al₂O₃. Likewise the glass sealant composition may be free ofMgO (0 wt %), but preferably it contains up to 10 wt % MgO, such as0.5-4 wt % MgO. The glass sealant composition may be free (0 wt %) ofNa₂O+K₂O, but preferably it contains up to 2 wt % Na₂O+K₂O. The glasscomposition may also be free (0 wt %) of functional elements selectedfrom TiO₂, ZrO₂, F, P₂O₅, MoO₃, Fe₂O₃, MnO₂, La—Sr—Mn—O perovskite (LSM)and combinations thereof, but it may contain up to 5 wt % of these.

Preferably, the content of SiO₂, Al₂O₃, CaO and MgO represents 85-95 wt% or 87-97 wt % of the glass sealant composition, while the content ofNa₂O+K₂O and B₂O₃ represents 5-12 wt % of the glass sealant composition,and functional elements selected from TiO₂, F, ZrO₂, P₂O₅, MoO₃, Fe₂O₃,MnO₂ and La—Sr—Mn—O perovskite (LSM) and combinations thereof represent0-5 wt %.

As such, the invention encompasses the use of glass with composition50-70 wt % SiO₂, 0-20 wt % Al₂O₃, 10-50 wt % CaO, 0-10 wt MgO, 0-2 wt %(Na₂O+K₂O), 5-10 wt % B₂O₃, and 0-5 wt % of functional elements selectedfrom TiO₂, ZrO₂, F, P₂O₅, MoO₃, Fe₂O₃, MnO₂, La—Sr—Mn—O perovskite (LSM)and combinations thereof, as glass sealant in solid oxide fuel cellstacks.

In a particular embodiment of the invention the glass sealant is a glasswith composition: 52-56 wt % SiO₂, 12-16 wt % Al₂O₃, 16-25 wt % CaO, 0-6wt % MgO, 0-2 wt % Na₂O+K₂O, 5-10 wt % B₂O₃, 0-1.5 wt % TiO₂, 0-1 wt %F. This glass composition corresponds to the composition of E-glass andshows a thermal expansion coefficient of about 5.4·10⁻⁶ K⁻¹ from −30 to250° C. The TEC of interconnector plates is normally 12-13·10⁻⁶K⁻¹ andfor interconnector plates made of Inconnel 600 containing 18 wt % Cr, 8t % Fe with Ni as balance, the TEC may be as high as 17·10⁻⁶ K⁻¹. Assuch, the invention encompasses therefore also the use of E-glass withcomposition 52-56 wt % SiO₂, 12-16 wt % Al₂O₃, 16-25 wt % CaO, 0-6 wt %MgO, 0-2 wt % Na₂O+K₂O, 5-10 wt % B₂O₃, 0-1.5 wt % TiO₂, 0-1 wt % F asglass sealant in solid oxide fuel cell stacks.

A preferred E-glass composition is 55.11 wt % SiO₂, 15.85 wt % CaO, 4.20wt % MgO, 15.34 wt % Al₂O₃, 8.80 wt % B₂O₃, 0.39 wt % Na₂O, and 0.31 wt% K₂O. Another suitable E-glass composition is 55.50 wt % SiO₂, 19.80 wt% CaO, 1.80 wt % MgO, 14.00 wt % Al₂O₃, 8.00 wt % B₂O₃, 0.90 wt % Na₂O.

We have found that despite the significantly lower TEC of the sealingmaterial in the first fuel cell stack assembly of step (a), it ispossible to prepare a final fuel cell stack in which the TEC of thecomponents including the sealant work well together without creation ofleakages during normal operation and thermal cycling. It appears thatthe sealant is kept under compression during the cooling step (c) due tothe larger contraction in the interconnector plate and the cell duringthis stage. A calculation based on an elastic fracture mechanical modelwhich takes into consideration the non-linearity of the thermalexpansion coefficient using a TEC of 13.3·10⁻⁶ K⁻¹ (RT-700° C.) for theinterconnect plates and the cells, and 6·10⁻⁶ K⁻¹ for a glass sealantaccording to the invention with thickness 11-33 μm and forming 10% ofthe stack shows that the maximum energy release rate for the glasslayers is 20 J/m², which is close to the maximum release rate of thecell (18 J/m²). Hence, no cracking of the cells takes place due to theformation of the very thin glass sealant, i.e. 5-100 μm and in thisparticular case 11-33 μm.

In the heating step (b) the first fuel cell stack assembly is morepreferably heated to 850-900° C. and maintained at this temperature forhold times of 2 to 6 hours. At these hold times and even after about 10hours no significant crystallization of the sealant occurs. However,after prolonged heating, for instance after about 84 hr at 850° C.,crystallization takes place and the TEC of the sealant surprisinglyincreases up to 10·10⁻⁶ K⁻¹ as measured in the range 25-800° C.

The glass sealant may or may not crystallize during the heating step (b)depending on the temperature and hold time used. Crystallization isinevitable during operation over more than 100 h at any temperatureequal or above 800° C. For instance, after 168 h of heat treatment at800° C. crystallisation of the sealant takes place in a compositionsimilar to that obtained at 850° C. for a hold time of 84 hours,resulting in a TEC up to 10·10⁻⁶ K₁ as measured in the range 25-800° C.The crystallizing phases of the sealant, particularly when using asealant having E-glass composition as recited above, is diopside rangingin composition from diopside to wollastonite, anorthite andcristobalite, while the B₂O₃ may stay in the glass phase. When MgO ispresent in the glass diopside (CaMg)Si₂O₆ may crystallize as the firstfase. The pseudowollastonite/wollastonite (CaSiO₃) crystallizes aroundthe diopside core. Anorthite CaAl₂Si₂O₈ form a solid solution serieswith albite, NaAlSi₃O₈, when Na₂O is present in the melt. A limitedamount of K₂O may also be included. The unexpectedly high TEC in thecrystallized sealant appears to be the result of the formation of thediopside-wollastonite (TEC about 8·10⁻⁶K⁻¹) and cristobalite (TEC about20·10⁻⁶K⁻¹), which counteract the presence of the low TEC anorthite (TECabout 5·10⁻⁶ K⁻¹).

The crystallized sealant imposes less tensile force onto the ceramiccell and thus reduces the risk of crack formation.

Accordingly, the sealant has a better match with the rest of the fuelcell, particularly the interconnect, and the risk for fuel cell crackingduring thermal cycling is further suppressed.

In order to ensure a fast crystallization of the sealant, nucleationelements such as Pt, F, TiO₂, ZrO₂, MoO₃, LSM and Fe₂O₃ can be added.

The sealant is poor in alkali components given by the sum Na₂O+K₂O, andis free of BaO. Normally a low (<2 wt %) alkali content of the sealantensures a low electrical conductivity. Furthermore, alkali elements insignificant amounts are corrosive to the Cr-rich oxide scale ofinterconnects made of chromium based alloys by forming Na₂CrO₄ having amelting point of 792° C., K₂CrO₄ having a melting point of 976° C., or(Na,K)₂CrO₄ with a minimum melting point of 752° C. These componentsbecome mobile at 800° C. and electrically conductive when operating atthis temperature. The alkaline earth BaO used in the prior art toincrease the TEC may also be corrosive to the Cr-oxide scale formingBaCrO₄ which may generate detachment cracks.

In another embodiment of the invention the glass sealant in step (a) isprovided as a sheet of glass fibres.

As used herein the term “sheet of glass fibres” defines a layer 0.10 to1.0 mm thick of glass fibres applied in step (a) and which correspondsto a 5 to 100 μm thick dense sealant layer after treatment according tothe invention. The sheet of glass fibres is preferably fibre glasspaper, more preferably E-glass paper such as fibre glass papercontaining or loaded with fibres in an amount ranging from 20 to 200g/m², preferably 30 to 100 g/m², such as 50 to 100 g/m²

Preferably, the sheet of glass fibres contains fibres in an amount of100 to 200 g/m² towards the cell unit and 20 to 50 or 60 g/m² towardsthe interconnect plate. More preferably, the sheet of glass fibrescontains fibres in an amount of 70-100 g/m², such as 100 g/m² towardsthe cell and 30-60 g/m², such as 50 g/m² towards the interconnect platecorresponding to about 40 and 20 μm thick dense sealant layer aftertreatment according to the invention. Most preferably, the sheet ofglass fibres is E-glass paper and contains fibres in an amount of 70-100g/m², such as 100 g/m² towards the cell and 30-60 g/m², such as 50 g/m²towards the interconnect plate corresponding to about 40 and 20 μm thickdense sealant layer after treatment according to the invention. Morespecifically, using for instance 80 g/m² towards the cell results in asealant thickness of about 30 μm and 30 g/m² towards the interconnectresults in a thickness of about 10 μm. By providing differentthicknesses of the sheet of glass fibres towards the cell and towardsthe interconnect plate, a superior sealing of the resulting SOFC stackis achieved.

The provision of the sealant as a sheet of glass fibres, for instance asa gasket of glass fibres, such as E-glass fibres, results in improvedthickness tolerance compared to fuel cell stacks in which the sealant isprovided as powder. The thickness of the sealant in the final fuel cellstack of 5-100 μm, preferably 5-50 μm, is kept within a specified narrowrange such as ±5 μm. Thus, disparities in the thickness of the sealantbetween the fuel cell units of the final fuel cell stack are eliminatedor at least significantly reduced compared to fuel cell stacks in whichthe sealant is provided by conventional spraying or deposition of aslurry or paste pre-pared from e.g. powder. Further, the provision ofthe sealant in step (a) as a sheet of glass fibres enables that thesolid oxide fuel cell stack comprising the sealant can be made by simplepunching commercial available E-glass fibre bands without resorting tomuch more expensive alternatives such as the implementation ofprocessing steps connected with the production of glass powder into aslurry or a paste to form the sealant or the addition of filler materialto increase the TEC of the sealant.

The sheet of glass fibres may be provided as chopped E-glass fibres suchas commercial E-glass in the form of sheets of 0.10-1.0 mm, preferably0.3-1.0 mm in thickness, corresponding to a thickness of the sealant inthe final fuel cell stack of 5-50 μm, often 10-40 μm, more often 10-35μm, such as 20 μm and particularly 11-33 μm. The sheet of E-glass fibresis commercially available (e.g. E-glass of 50-100 g/m²) and represents asimple and inexpensive solution to the problem of providing propersealants in fuel cell stacks, i.e. sealants which during operationsuppress fuel cell cracking, which are gas-tight, which provideelectrical isolation of the cell and which present low reactivity withinterconnector plates. When using E-glass as the starting glassmaterial, this E-glass is also preferably provided as a sheet of glassfibres, such as E-glass fibre paper. Because E-glass may be delivered asrolls of glass fibres, the shape of the sealant with corresponding holesfor the separate passage of fuel or oxidant can be provided efficientlyand expediently by simple punching methods.

In yet another embodiment the sealant in step (a) is loaded with fillermaterial in the form of MgO, steel-powder, quartz, leucite andcombinations thereof. The high TEC of the filler material enables toobtain a composite glass sealant with a TEC corresponding to that of theinterconnect plate i.e. 12-13·10⁻⁶ K⁻¹.

In another embodiment the glass sealant is a paste formed by mixing aglass powder having the composition recited in claim 1 with a binder andan organic solvent. The paste is used for screen printing or as a pasteto be used in a dispenser to make a sealant.

The glass powder may be mixed with a filler in the form of MgO,steel-powder, quartz, leucite and combinations thereof in order toproduce a glass having TEC of 12-13·10⁻⁶ K⁻¹.

Once again and regardless of whether the glass is provided as a sheet ofglass fibres or as a paste, by the invention it is possible to convertthe starting glass fibre material into a thin glass sealant, i.e. 5-100μm, often 5-50 μm, preferably 11-33 μm, in the final fuel cell stackwhich is dense and thereby gas-tight, i.e. hermetic. This is highlydesirable since a hermetic sealant serves to prevent the mixing of thefuel in the anode and the oxidant in the cathode in adjacent fuel cellunits. The hermeticity appears to be the result of a completecoalescence between the individual fibres squeezed together by the loadexerted on the cell stack during the heating step (b) and the use of atemperature during this step which often is at least equal to thesoftening point of the glass sealant (above 800° C.). A closed porestructure or a dense glass is thereby obtained. The relatively highsoftening temperature of the sealant (above about 800° C.) enables thatthe sealant maintains a high viscosity, such as 10⁹-10¹¹ Pa-s at theoperating temperatures of the fuel cell stack, for instance at 750-800°C.

FIG. 1 shows a window of 21 thermal cyclings recorded during operationof a ten-cell stack prepared according to the invention within anoverall period of 26 days (units of two days).

FIG. 2 shows the OCV (open circuit voltage) profile in terms of averagevalues over a period of 40 days (units of 5 days).

EXAMPLE 1

An anode supported cell 300 μm thick with internal feeding and exhaustholes has demasked contact layers in the manifold areas in order tominimise leakage through these porous structures. A metal gasket framecovered with equally shaped punched E-glass fibre paper on both sides isplaced on both sides of the cell in such a way that air from themanifold holes is allowed to pass over the cathode and fuel gas isallowed to pass over the anode side. Above and below the cell and gasketassemblage is placed an interconnect plate with manifold holes. TheE-glass paper contains fibres in an amount of 100 g/m² towards the celland 50 g/m² towards the interconnect plate corresponding to,respectively, 40 and 20 μm thick dense layer after treatment accordingto the invention at temperatures of about 880° C. and load pressure ofabout 6 kg/cm². Building a stack with 5 cells, cross-over leak betweenthe anode and cathode sides has been measured at RT to as low as 0.05and 0.09% in two stacks after a full thermal cycle. With gaschromatography using steps of 2×N₂ conc. in oxygen on the cathode sideand measuring the N₂ mole conc. on the anode side during operation withthe same gas pressure on the anode and cathode side we obtained adoubling of the N₂ mole % in the anode of each step showing that thethere is a leakage and that it is diffusion driven, presumably due tothe diffusion through the porous structures of the cell (mainly theanode support). Increasing the gas pressure on the cathode side did nothave any effect on the cross-over leak on the anode side.

XRD-spectres of the E-glass show the presence of wollastonite, CaSiO₃(diopside, (Ca,Mg)SiO₃ also fit the spectrum and its presence isdependent on the MgO-content of the glass) together with anorthite(CaAl₂Si₂O₈, which may contain up to 10 moles NaAlSi₃O₈) andcristobatite, (SiO₂)

Thermal cycling 21 times during operation or removal of a ten-cell stackto other test facilities (FIG. 1) does not have any significant effecton the cross-over leak between the fuel side and air side of the cellsas can be seen in the OCV (open circuit voltage) (FIG. 2). The flat OCVprofile of FIG. 2 shows that the invention enables to prepare by simplemeans (use of E-glass fibre paper as glass sealant precursor) a finalfuel cell stack in which the components of the stack including thesealant work well together without creation of leakages during normaloperation and thermal cycling. In addition, no deteriorating reactionsoccur between the oxide scale and the E-glass.

Similar flat OCV profiles are obtained in the subsequent examples:

EXAMPLE 2

As Example 1, but the E-glass sealant is infiltrated (by dip coating orspraying) or with a slurry containing 20-50 volt 1-5 μm sized MgOgrains, 3′ PVA and 67 volt ethanol.

EXAMPLE 3

As Example 2: where the slurry contain 20-50 vol % of 1-3 μm AISI 316Lpowder.

EXAMPLE 4

As example 2: where the slurry contains 20-50 vol % of leucite.

EXAMPLE 5

E-glass is produced from dry mixing of the oxides in a ball mill to givethe composition below, in a ball mill and melting the mixture in a Ptcrucible at 1500° C. for two hours. The crucible is then quenched inwater or liquid N₂ followed by crushing and grounding the sample to agrain size of <10 μm. A paste is then prepared which suitable for use ina dispenser or as a paste for screen printing.

Wt % SiO2 55.11 CaO 15.85 MgO 4.20 Al2O3 15.34 B2O3 8.80 Na2O 0.39 K2O0.31 100.00

EXAMPLE 6

Making the E-glass with the composition below from a sol-gel route: a92.4 g 30 wt % silica sol (Ludox) is mixed with 9.29 g B₂CaO₄+6.68 gCa(NO₃)₂*4H₂O+25.75 g Al(NO₃)₃*9H₂O+5.73 g Mg(NO₃)₂*6H₂O+0.53 g Na₂CO₃.The mixture forms a gel which by calcination to 730° C. forms a glasswith tiny crystals of wollastonite and cristobalite according to XRD.The glass is easily crushed and ground to specific size. The gel is usedas a paint or a paste for a dispenser or screen printing.

Wt % SiO2 55.50 CaO 19.80 MgO 1.80 Al2O3 14.00 B2O3 8.00 Na2O 0.90 K2O0.00 100.00

1. Solid oxide fuel cell stack obtainable by a process comprising thesteps of: (a) forming a first fuel cell stack assembly by alternating atleast one interconnector plate with at least one fuel cell unit, inwhich each fuel cell unit comprises an anode, a cathode and anelectrolyte arranged between the anode and cathode, and providing aglass sealant in between the interconnector plate and each fuel cellunit, in which the glass sealant has the composition: 50-70 wt % SiO₂,0-20 wt % Al₂O₃, 10-50 wt % CaO, 0-10 wt % MgO, 0-2 wt % (Na₂O+K₂O),5-10 wt % B₂O₃, and 0-5 wt % of functional elements selected from TiO₂,ZrO₂, F, P₂O₅, MoO₃, Fe₂O₃, MnO₂, La—Sr—Mn—O perovskite (LSM) andcombinations thereof; (b) converting said first fuel cell stack assemblyinto a second assembly having a glass sealant of thickness 5-100 μm byheating said first assembly to a temperature of 500° C. or higher andsubjecting the cell stack to a load pressure of 2 to 20 kg/cm²; (c)converting said second assembly into a final fuel cell stack assembly bycooling the second assembly of step (b) to a temperature below that ofstep (b).
 2. Solid oxide fuel cell stack obtainable by a processcomprising the steps of: (a) forming a first fuel cell stack assembly byalternating at least one interconnector plate with at least one fuelcell unit, in which each fuel cell unit comprises an anode, a cathodeand an electrolyte arranged between the anode and cathode, and providinga glass sealant in between the interconnector plate and each fuel cellunit in which the gas sealant has the composition: 50-70 wt % SiO₂, 0-20wt % Al₂O₃, 10-50 wt % CaO, 0-10 wt % MgO, 0-2 wt % (Na₂O+K₂O), 5-10 wt% B₂O₃, and 0-5 wt % of functional elements selected from TiO₂, ZrO₂, F,P₂O₅, MoO₃, Fe₂O₃, MnO₂, La.Sr—Mn—O perovskite (LSM) and combinationsthereof; (b) converting said first fuel cell stack assembly into asecond assembly having a glass sealant of thickness 5-100 μm by heatingsaid first assembly to a temperature of 800° C. or higher and subjectingthe cell stack to a load pressure of 2 to 10 kg/cm², (c) converting saidsecond assembly into a final fuel cell stack assembly by cooling thesecond assembly of step (b) to a temperature below that of step (b). 3.Solid oxide fuel cell stack according to claim 1, wherein the content ofSiO₂, Al₂O₃, CaO and MgO represents 85-95 wt % of the glass sealantcomposition, the content of Na₂O+K₂O and B₂O₃ represents 5-12 wt % ofthe glass sealant composition and functional elements selected fromTiO₂, F, ZrO₂, P₂O₅, MoO₃, Fe₂O₃, MnO₂ and La.Sr—Mn—O perovskite (LSM)and combinations thereof represent 0-5 wt %.
 4. Solid oxide fuel cellstack according to claim 1, wherein the glass sealant is a glass withcomposition: 52-56 wt % SiO₂, 12-16 wt % Al₂O₃, 16-25 wt % CaO, 0-6 wt %MgO, 0-2 wt % Na₂O+K₂O, 5-10 wt % B₂O₃, 0-1.5 wt % TiO₂, 0-1 wt % F. 5.Solid oxide fuel cell stack according to claim 1, wherein the glasssealant in step (a) is provided as a sheet of glass fibres.
 6. Solidoxide fuel cell stack according to claim 1, wherein the sheet of glassfibres contains fibres in an amount of 70-100 g/m² towards the cell and30-60 g/m² towards the interconnect plate.
 7. Solid oxide fuel cellstack according to claim 1, wherein the glass sealant in step (a) isloaded with filler material in the form of MgO, steel-powder, quartz,leucite and combinations thereof.
 8. Solid oxide fuel cell stack,wherein the glass sealant is a paste formed by mixing a glass powderhaving the composition of claim 1 with a binder and an organic solvent.9. Solid oxide fuel cell stack according to claim 8, wherein the glasspowder is mixed with a filler material in the form of MgO, steel-powder,quartz, leucite and combinations thereof.
 10. Use of E-glass withcomposition 52-56 wt % SiO₂, 12-16 wt % Al₂O₃, 16-25 wt % CaO, 0-6 wt %MgO, 0-2 wt % Na₂O+K₂O, 5-10 wt % B₂O₃, 0-1.5 wt % TiO₂, 0-1 wt % F asglass sealant in solid oxide fuel cell stacks.
 11. Use according toclaim 10 wherein the glass is provided as a sheet of glass fibres. 12.Use according to claim 11 wherein the sheet of glass fibres containsfibres in an amount of 70-100 g/m² towards the cell and 30-60 g/m²towards the interconnect plate.